HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249607Generated: October 27, 2026
Hydrochloric Acid → HCID 178452996, compound
https://huagongshe.com/reaction/249607
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Phosphorodichloridic acid, phenyl ester | HCID 13038 | — |
| Reactant | 2-(2-((Tert-butoxycarbonyl)amino)thiazol-4-yl)-2-oxoacetic acid | HCID 14852119 | — |
| Reactant | HCID 178511753 | HCID 178511753 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178452996 | HCID 178452996 | 63.5% |
Reaction Steps
To a solution of 7β-amino-3-(trityl-1,2,3-triazol-4-ylthiomethylthio) -3-cephem-4-carboxylic acid diphenylmethyl ester (800 mg : 1.06 mMol.) and 2-(2-t-butoxycarbonylaminothiazol-4-yl) glyoxylic acid (303 mg : 1.11 mMol.) in dichloromethane (8 ml) cooling at -30° C., are added N- methylmorpholine (0.27 ml) (2.46 mMol.) and phenyl dichlorophosphate (0.19 ml : 1.27 mMol.), and the mixture is stirred at -30° C. for 1 hour. The reaction mixture is mixed with 10% hydrochloric acid (1 ml), diluted with water, and extracted with ethyl acetate. The extract is washed with brine, dried over sodium sulfate, and concentrated. The residue is purified by silica gel chromatography (toluene : ethyl acetate=2:1) to give 7β-[2-(2-t-butoxycarbonylaminothiazol-4-yl)- glyoxylylamino]-3-(trityl-1,2,3-triazol-4-ylthiomethylthio) -3-cephem-4- carboxylic acid diphenylmethyl ester (679 mg) as yellow foam. Yield : 64%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05214037 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-c2b3f179427f49c9bd1a126ae724a77b |
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| Source note | uspto-grants-1993_05 |
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